| Primary Device ID | 00887761970106 |
| NIH Device Record Key | 95daa931-3376-49e4-b638-52bf01692e72 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Carbon Sections |
| Version Model Number | 2077576 |
| Company DUNS | 330961223 |
| Company Name | Baxter Medical Systems GmbH + Co. KG |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +4936715860 |
| SURGICAL@HILLROM.COM | |
| Phone | +4936715860 |
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| Phone | +4936715860 |
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| Phone | +4936715860 |
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| Phone | +4936715860 |
| SURGICAL@HILLROM.COM | |
| Phone | +4936715860 |
| SURGICAL@HILLROM.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887761970106 [Primary] |
| JEA | TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED |
| KXJ | Table, radiologic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-02-09 |
| Device Publish Date | 2022-12-14 |
| 00887761970939 | Table top segment Carbon 600 H V |
| 00887761970328 | 1850989 |
| 00887761970106 | Carbon 600 Narrow H |
| 00887761967410 | Carbon 450 H |